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Structure of 633283-63-3
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tert-Butyl 4-(2-chloropyridin-4-yl)piperazine-1-carboxylate features a chloropyridine moiety coupled to a piperazine scaffold, enabling direct incorporation into kinase inhibitors and bioactive heterocycles. The tert-butyl ester group provides stability and facilitates deprotection under mild acidic conditions. This compound serves as a key intermediate in the synthesis of pharmaceutical candidates targeting receptor tyrosine kinases.
tert-Butyl 4-(2-chloropyridin-4-yl)piperazine-1-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridyl-piperazine scaffolds commonly found in kinase inhibitors and CNS-targeted therapeutics. The tert-butyl carbamate group offers excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The 2-chloropyridine moiety provides a reactive handle for palladium-catalyzed cross-coupling reactions, including Suzuki and Buchwald-Hartwig amination, supporting diverse structural elaboration in lead optimization campaigns.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: